Citation: Dn. Chen et al., Minimal regions of chromosomal imbalance in retinoblastoma detected by comparative genomic hybridization, CANC GENET, 129(1), 2001, pp. 57-63
Authors:
Wong, KF
So, CC
Wong, N
Siu, LLP
Kwong, YL
Chan, JKC
Citation: Kf. Wong et al., Sinonasal angiosarcoma with marrow involvement at presentation mimicking malignant lymphoma: cytogenetic analysis using multiple techniques, CANC GENET, 129(1), 2001, pp. 64-68
Authors:
Ishii, E
Kimura, N
Honda, K
Eguchi, M
Nakayama, H
Tanaka, M
Ichinose, I
Yoshida, T
Tamura, K
Citation: E. Ishii et al., Oligoclonal expansion of alpha beta T lymphocytes in Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis with abnormal karyotypes, CANC GENET, 129(1), 2001, pp. 69-75
Authors:
Emberger, W
Behmel, A
Tschernigg, M
Seewann, HL
Petek, E
Kroisel, PM
Wagner, K
Citation: W. Emberger et al., Chronic myeloid leukemia with a rare variant Philadelphia translocation: t(9;10;22)(q34;q22;q11), CANC GENET, 129(1), 2001, pp. 76-79
Authors:
Kahl, C
Gesk, S
Harder, L
Harbott, J
French, L
Deloukas, P
Grote, W
Schlegelberger, B
Siebert, R
Citation: C. Kahl et al., Detection of translocations involving the HOX11/TCL3-locus in 10q24 by interphase fluorescence in situ hybridization, CANC GENET, 129(1), 2001, pp. 80-84
Authors:
Varley, JM
McGown, G
Thorncroft, M
Kelsey, AM
Birch, JM
Citation: Jm. Varley et al., Significance of intron 6 sequence variations in the TP53 gene in Li-Fraumeni syndrome, CANC GENET, 129(1), 2001, pp. 85-87
Authors:
Vieira, L
Oliveira, V
Ambrosio, AP
Marques, B
Pereira, AM
Hagemeijer, A
Boavida, MG
Citation: L. Vieira et al., Translocation (8;17;15;21)(q22;q23;q15;q22) in acute myeloid leukemia (M2): a four-way variant of t(8;21), CANC GENET, 128(2), 2001, pp. 104-107
Authors:
Stark, B
Jeison, M
Gobuzov, R
Krug, H
Glaser-Gabay, L
Luria, D
El-Hasid, R
Ben Harush, M
Avrahami, G
Fisher, S
Stein, J
Zaizov, R
Yaniv, I
Citation: B. Stark et al., Near haploid childhood acute lymphoblastic leukemia masked by hyperdiploidline: detection by fluorescence in situ hybridization, CANC GENET, 128(2), 2001, pp. 108-113
Authors:
Cohen, N
Rozenfeld-Granot, G
Hardan, I
Brok-Simoni, F
Amariglio, N
Rechavi, G
Trakhtenbrot, L
Citation: N. Cohen et al., Subgroup of patients with Philadelphia-positive chronic myelogenous leukemia characterized by a deletion of 9q proximal to ABL gene: expression profiling, resistance to interferon therapy, and poor prognosis, CANC GENET, 128(2), 2001, pp. 114-119
Authors:
Summersgill, BM
Jafer, O
Wang, R
Goker, H
Niculescu-Duvaz, I
Huddart, R
Shipley, J
Citation: Bm. Summersgill et al., Definition of chromosome aberrations in testicular germ cell tumor cell lines by 24-color karyotyping and complementary molecular cytogenetic analyses, CANC GENET, 128(2), 2001, pp. 120-129
Authors:
Martins, C
Fonseca, I
Roque, L
Ribeiro, C
Soares, J
Citation: C. Martins et al., Cytogenetic similarities between two types of salivary gland carcinomas: adenoid cystic carcinoma and polymorphous low-grade adenocarcinoma, CANC GENET, 128(2), 2001, pp. 130-136
Authors:
Walker, LC
Morrison, MJ
Parfitt, R
Crossen, PE
Citation: Lc. Walker et al., Translocation (2;14) associated with complex rearrangements of the Ig heavy chain in non-Hodgkin lymphoma, CANC GENET, 128(2), 2001, pp. 137-140
Authors:
Herishanu, Y
Lishner, M
Bomstein, Y
Kitay-Cohen, Y
Fejgin, MD
Gaber, E
Amiel, A
Citation: Y. Herishanu et al., Comparative genomic hybridization in polycythemia vera and essential thrombocytosis patients, CANC GENET, 128(2), 2001, pp. 154-157
Authors:
Odagaki, T
Sugimoto, T
Matsuo, M
Tatsumi, E
Saigo, K
Citation: T. Odagaki et al., Tetrasomy 21 as the sole acquired karyotypic abnormality in acute myeloblastic leukemia, CANC GENET, 128(2), 2001, pp. 158-160
Authors:
Sukosd, F
Digon, B
Fischer, J
Pietsch, T
Kovacs, G
Citation: F. Sukosd et al., Allelic loss at 10q23.3 but lack of mutation of PTEN/MMAC1 in chromophobe renal cell carcinoma, CANC GENET, 128(2), 2001, pp. 161-163
Authors:
Dierlamm, J
Stefanova, M
Wlodarska, I
Michaux, L
Hinz, K
Penas, EMM
Maes, B
Hagemeijer, A
De Wolf-Peeters, C
Hossfeld, DK
Citation: J. Dierlamm et al., Chromosomal gains and losses are uncommon in hairy cell leukemia: a study based on comparative genomic hybridization and interphase fluorescence in situ hybridization, CANC GENET, 128(2), 2001, pp. 164-167
Authors:
Guillaume, B
Ameye, G
Dierlamm, J
Verhoef, G
Duhem, C
Ferrant, A
Hagemeijer, A
Verellen-Dumoulin, C
Michaux, L
Citation: B. Guillaume et al., Trisomy 16 as the sole anomaly in hematological malignancies: three new cases and a short review, CANC GENET, 128(2), 2001, pp. 168-171
Authors:
Gancberg, D
Dargent, JL
Verhest, A
Kentos, A
Feremans, W
Lohrisch, C
Kornreich, A
Citation: D. Gancberg et al., Near-haploid blast phase in a chronic myeloid leukemia detected by fluorescence in situ hybridization using a BCR-ABL probe, CANC GENET, 128(2), 2001, pp. 172-174
Citation: J. Swan et al., Constitutional t(5;11)(p15.3;q23) in an adolescent male with acute lymphoblastic leukemia, CANC GENET, 128(2), 2001, pp. 178-180